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1.
J Int Med Res ; 41(5): 1639-47, 2013 Oct.
Article in English | MEDLINE | ID: mdl-24029022

ABSTRACT

OBJECTIVE: To compare unilateral spinal anaesthesia (USA) and ultrasound-guided combined sciatic-femoral nerve block (USFB) in ambulatory arthroscopic knee surgeries in terms of haemodynamic stability, nerve block quality, bladder function, adverse events and time-to-readiness for discharge (TRD). METHODS: Patients undergoing ambulatory arthroscopic knee surgery were randomly assigned to one of two groups. The USA group received 2 ml (10 mg) of 0.5% levobupivacaine and the USFB group received a 25 ml mixture consisting of 10 ml of 2.0% lidocaine, 10 ml of 0.5% levobupivacaine and 5 ml of saline (15 ml for the femoral and 10 ml for the sciatic nerve block). Preparation time (PT), surgical anaesthesia time (SAT), operation time, total anaesthesia time, time-to-first spontaneous urination, time-to-first analgesia, TRD, adverse events and patient satisfaction were recorded. RESULTS: A total of 40 patients were enrolled in the study (n = 20 per group). PT, SAT, total anaesthesia time and time-to-first analgesia were significantly shorter in the USA group than the USFB group; time-to-first spontaneous urination and TRD were significantly longer in the USA group than the USFB group. CONCLUSIONS: USFB provided sufficient duration of sensory blockade and it reduced the TRD and the rate of adverse events.


Subject(s)
Anesthesia, Spinal/methods , Anesthetics, Local , Arthroscopy , Bupivacaine/analogs & derivatives , Knee Joint/surgery , Lidocaine , Nerve Block/methods , Adult , Ambulatory Surgical Procedures , Female , Femoral Nerve/drug effects , Hemodynamics/physiology , Humans , Knee Joint/diagnostic imaging , Knee Joint/pathology , Levobupivacaine , Male , Middle Aged , Nerve Block/instrumentation , Outpatients , Sciatic Nerve/drug effects , Ultrasonography , Urinary Bladder/physiology
2.
Otolaryngol Head Neck Surg ; 138(2): 158-61, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18241708

ABSTRACT

OBJECTIVE: Hemorrhage during tonsillectomy is related to the surgical technique, management of bleeding, and choice of anesthetic agent. This study evaluated the effects of anesthetic agents on hemorrhage during tonsillectomy with standardized surgical techniques and management of bleeding. STUDY DESIGN: Double-blind, randomized controlled trial. SUBJECTS AND METHODS: Sixty patients, aged 3 to 12 years, who were scheduled for elective tonsillectomy were enrolled in the study. Propofol-based anesthesia was administered to the first group; desflurane-based anesthesia, to the second. The amount of blood loss due to hemorrhage was measured. RESULTS: Propofol-based anesthesia significantly decreased bleeding during tonsillectomy. CONCLUSION: Propofol-based anesthesia is a reliable method for use in children who undergo tonsillectomy.


Subject(s)
Anesthesia, General/methods , Anesthetics, Inhalation/administration & dosage , Anesthetics, Intravenous/administration & dosage , Blood Loss, Surgical/prevention & control , Isoflurane/analogs & derivatives , Propofol/administration & dosage , Tonsillectomy/methods , Administration, Inhalation , Adolescent , Child , Child, Preschool , Desflurane , Double-Blind Method , Elective Surgical Procedures , Female , Follow-Up Studies , Humans , Injections, Intravenous , Isoflurane/administration & dosage , Male , Neuroprotective Agents , Prospective Studies , Treatment Outcome
3.
J Clin Anesth ; 19(8): 587-90, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18083471

ABSTRACT

STUDY OBJECTIVE: To determine whether intravenous injection of lornoxicam 30 minutes before skin incision provides better pain relief after varicocelectomy than postoperative administration of lornoxicam. DESIGN: Prospective, double-blind, randomized clinical investigation. SETTING: Operating room and postoperative recovery area. PATIENTS: 44 ASA physical status I and II adult male patients undergoing varicocelectomy. INTERVENTIONS: Patients were randomized either to receive 8 mg lornoxicam infusion 30 minutes before skin incision, followed by saline infusion immediately after skin closure (group 1), or to receive the identical injections but in reverse order (group 2). All patients received local anesthesia with bupivacaine. MEASUREMENTS: Postoperative pain scores were evaluated hourly for the first 8 hours after surgery, then at 12, 16, 20, and 24 hours after surgery, using a 10-cm visual analog scale. Time to first analgesic request and patients' global assessments also were recorded. MAIN RESULTS: Patients in group 1 reported significantly lower pain scores (P < 0.05) at all time intervals except at 24 hours and better global assessment (P = 0.001) than did group 2. There were significantly fewer patients in the preemptive group than group 2 who required rescue analgesic within the first 24 hours (0% vs 22.7%; P = 0.024). Mean time to first analgesic request was also significantly longer in the preemptive group (P = 0.001). CONCLUSION: Intravenous lornoxicam administered before surgery has a better analgesic effect for varicocelectomy than when administered postoperatively.


Subject(s)
Analgesia/methods , Pain, Postoperative/drug therapy , Piroxicam/analogs & derivatives , Postoperative Care/methods , Preoperative Care/methods , Varicocele/surgery , Adult , Ambulatory Surgical Procedures/methods , Anesthesia, Local/methods , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Double-Blind Method , Humans , Injections, Intravenous , Male , Pain Measurement/statistics & numerical data , Pain, Postoperative/prevention & control , Piroxicam/administration & dosage , Piroxicam/therapeutic use , Prospective Studies , Sodium Chloride/administration & dosage , Time Factors , Treatment Outcome
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